EA 4267 Fonctions et Dysfonctions Epitheliales

Besançon, France

EA 4267 Fonctions et Dysfonctions Epitheliales

Besançon, France
SEARCH FILTERS
Time filter
Source Type

Devaux S.,EA 4267 Fonctions et dysfonctions epitheliales | Adrian M.,EA 4267 Fonctions et dysfonctions epitheliales | Laurant P.,EA 4267 Fonctions et dysfonctions epitheliales | Berthelot A.,EA 4267 Fonctions et dysfonctions epitheliales | Quignard-Boulange A.,French National Institute for Agricultural Research
Magnesium Research | Year: 2016

Obesity and related metabolic diseases are associated with increased risk of cardiovascular disease. We have previously shown the beneficial effects of dietary magnesium (Mg) supplementation on cardiovascular disease in rats. Therefore, we aimed to examine the effect of an Mg-deficient or supplemented diet on adipose tissue cellularity changes during aging, and on blood pressure (BP), in rats. Male rats received for one (young adult) or 22 months (old), an Mgdeficient (Def) (150 mg/kg), standard (Std) (800 mg/kg) or Mg-supplemented (Sup) (3200 mg/kg) diet. Adipose tissue development and cellularity, BP and leptinemia were evaluated. In rats fed a standard diet, the large increase in adipose tissue weight observed during aging was related to an increase in both size and number of adipocytes. In young adult rats, although adiposity was unchanged, Mg supplementation resulted in a shift of the frequency distribution of adipocytes toward greater sizes, adipose cell weight increasing by 62%. Mg deficiency did not modify adipocyte size, but increased their number (30% more than for the standard or Sup-diet). In old rats, the Def-diet led to relative adipocyte hypotrophy, which was counterbalanced by an increase in the number of adipocyte. Conversely, adipocyte size and number were similar in the Supdiet and standard diet-fed rats. BP was modified in old rats according to dietary Mg, whereas it remained unchanged young adult rats regardless of the diet received. This study suggests that Mg intake may affect age-related changes in rat adipose tissue lipid storage capacity. © 2017 John Libbey Eurotext.


Tom E.N.L.,EA 4267 Fonctions et Dysfonctions Epitheliales | Tom E.N.L.,Mohammed V University | Girard-Thernier C.,EA 4267 Fonctions et Dysfonctions Epitheliales | Martin H.,EA 4267 Fonctions et Dysfonctions Epitheliales | And 5 more authors.
Journal of Ethnopharmacology | Year: 2014

Ethnopharmacological relevance The stem bark of Terminalia superba (TS) is widely used as a decoction by Cameroonian folk medicine for the treatment of hypertension. The aim of the present study was to evaluate the effect of a chronic treatment with a TS extract on spontaneously hypertensive rats (SHR) with respect to efficacy, biochemical mechanisms and safety. Materials and methods Eleven-week-old SHR and normotensive Wistar Kyoto rats (WKY) were daily treated by gavage with a methylene chloride extract of stem bark of Terminalia superba (TMSE, 150 mg/kg) or with the vehicle for 5 weeks. Systolic blood pressure (SBP) was measured weekly using the tail-cuff method. At the end of the treatment period, vascular function was assessed on isolated thoracic rings, urinary 8-iso-PGF2α levels were measured and cytochrome P-450 3A (CYP 3A) activity was evaluated in liver microsomes. Results TMSE reduced SBP (P<0.001) in SHR but not in WKY rats. In SHR, the vasorelaxant response to acetylcholine was significantly improved by TMSE as a result of increased nitric oxide synthase (NO) activity and decreased superoxide anion production. In addition, TMSE reduced the vasoconstrictive effect of phenylephrine and improved the sensitivity of smooth muscle cells to NO. TMSE dramatically decreased 8-iso-PGF2α levels in SHR. By contrast, TMSE did not affect all these parameters in WKY rats. Neither diuresis nor the hepatic CYP 3A activity was modified in both animal groups. Conclusions This study demonstrated that Terminalia superba has a potent antihypertensive activity in SHR which is partly due to endothelium-dependent and endothelium-independent effects as well as decreased oxidative stress. The data also provide evidence for the lack of herb-drug interaction through hepatic CYP 3A. © 2013 Elsevier Ireland Ltd.


Senejoux F.,EA 4267 Fonctions et Dysfonctions Epitheliales | Demougeot C.,EA 4267 Fonctions et Dysfonctions Epitheliales | Cuciureanu M.,Grigore T. Popa University of Medicine and Pharmacy | Miron A.,Grigore T. Popa University of Medicine and Pharmacy | And 3 more authors.
Journal of Ethnopharmacology | Year: 2013

Ethnopharmacological relevance Aerial parts of Heracleum sphondylium L. (HS) are used in traditional medicine to treat hypertension. To provide pharmacological basis for this use, we investigated the vasorelaxant effects of a dichloromethane extract of HS (HSDE) and the mechanisms involved. Materials and methods Activity of HSDE was evaluated on rat isolated thoracic aortic rings. Results HSDE induced vasorelaxation in phenylephrine (PE, 10-6 mol/L) and high KCl - (6×10-2 mol/L) pre-contracted aortic rings that was independent on the presence of endothelium. HSDE markedly decreased extracellular Ca2+-induced contraction in high-KCl and PE pre-challenged rings. It also inhibited the intracellular Ca2+ release sensitive to PE (10-6 M). The relaxant effect of HSDE were blunted by 4-amino-pyridine (4-AP, 10-3 mol/L), an inhibitor of voltage-dependent K+ channels. Conclusion Our results provide the first evidence that a dichloromethane extract of Heracleum sphondylium L. exhibits vasorelaxant properties through endothelium-independent mechanisms involving the inhibition of Ca2+ mobilization and changes in Kv channel conductances. These data argue for its use as antihypertensive therapy in traditional medicine. © 2013 Elsevier Ireland Ltd. All rights reserved.


Laroche D.,French Institute of Health and Medical Research | Joussain C.,University Hospital of Dijon | Espagnac C.,French Institute of Health and Medical Research | Morisset C.,French Institute of Health and Medical Research | And 5 more authors.
Archives of Physical Medicine and Rehabilitation | Year: 2013

Objective: To assess the safety and acute effects of a procedure using perceived exertion during a prior submaximal concentric (CON) test to individualize eccentric (ECC) cycling exercise intensity. Design: Prospective, monocentric open study. Setting: Technological investigation platform at a physical medicine and rehabilitation department in a university hospital. Participants: Healthy subjects (N=18; 15 men, 3 women) aged between 22 and 37 years. Interventions: The subjects performed 3 cycling exercises: (1) incremental CON test to determine the comfortable pedaling power (CPP) corresponding to a Borg scale rating of 12 (rate of perceived exertion); (2) steady-state CON exercise at the CPP workload to determine the corresponding plantar pressure; and (3) steady-state ECC exercise with an imposed resistance corresponding to the CPP plantar pressure. Main Outcome Measures: Rate of perceived exertion on Borg scale, oxygen uptake (V̇o2), heart rate, cardiac output, and stroke volume using inert gas rebreathing techniques were measured during steady-state CON and ECC exercises. Muscle soreness was rated on a visual analog scale immediately, 24, and 48 hours after the tests. Results: No adverse effects were reported. V̇o2 was about 5 times the resting value during CON exercise, while it was twice that during ECC exercise. Cardiac output was lower during ECC exercise (P<.05). This moderate increase of cardiac output was exclusively linked to a greater increase in stroke volume during ECC exercise than during CON exercise (P<.05). Conclusions: Moderate-intensity ECC cycling exercise tailored according to perceived exertion during a prior CON test is well tolerated. It corresponds to a limited muscular use of oxygen and to an isolated increase in stroke volume. It appears to be a feasible procedure for preconditioning before ECC training. © 2013 by the American Congress of Rehabilitation Medicine.


Quirie A.,French Institute of Health and Medical Research | Quirie A.,University of Burgundy | Hervieu M.,French Institute of Health and Medical Research | Hervieu M.,University Hospital | And 12 more authors.
PLoS ONE | Year: 2012

Physical exercise constitutes an innovative strategy to treat deficits associated with stroke through the promotion of BDNF-dependent neuroplasticity. However, there is no consensus on the optimal intensity/duration of exercise. In addition, whether previous stroke changes the effect of exercise on the brain is not known. Therefore, the present study compared the effects of a clinically-relevant form of exercise on cerebral BDNF levels and localization in control versus stroke rats. For this purpose, treadmill exercise (0.3 m/s, 30 min/day, for 7 consecutive days) was started in rats with a cortical ischemic stroke after complete maturation of the lesion or in control rats. Sedentary rats were run in parallel. Mature and proBDNF levels were measured on the day following the last boot of exercise using Western blotting analysis. Total BDNF levels were simultaneously measured using ELISA tests. As compared to the striatum and the hippocampus, the cortex was the most responsive region to exercise. In this region, exercise resulted in a comparable increase in the production of mature BDNF in intact and stroke rats but increased proBDNF levels only in intact rats. Importantly, levels of mature BDNF and synaptophysin were strongly correlated. These changes in BDNF metabolism coincided with the appearance of intense BDNF labeling in the endothelium of cortical vessels. Notably, ELISA tests failed to detect changes in BDNF forms. Our results suggest that control beings can be used to find conditions of exercise that will result in increased mBDNF levels in stroke beings. They also suggest cerebral endothelium as a potential source of BDNF after exercise and highlight the importance to specifically measure the mature form of BDNF to assess BDNF-dependent plasticity in relation with exercise. © 2012 Quirié et al.


Totoson P.,EA 4267 Fonctions et Dysfonctions Epitheliales | Maguin-Gate K.,EA 4267 Fonctions et Dysfonctions Epitheliales | Prati C.,EA 4267 Fonctions et Dysfonctions Epitheliales | Prati C.,Besancon University Hospital Center | And 2 more authors.
Arthritis Research and Therapy | Year: 2014

Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease characterized by articular and extra-articular manifestations involving cardiovascular diseases (CVDs), which account for 30% to 50% of all deaths. In patients with RA, atherosclerosis lesions occur earlier and have a more rapid evolution than in the general population. Beyond mortality, the impact of CVD on quality of life, combined with the associated increase in health-care costs, renders CVD in RA a major public health problem. Recent studies showed that patients with RA are characterized by the presence of endothelial dysfunction (ED), which is recognized as a key event in the development of atherosclerosis. By definition, ED is a functional and reversible alteration of endothelial cells, leading to a shift of the actions of the endothelium toward reduced vasodilation, proinflammatory state and proliferative and prothrombotic properties. Although the improvement of endothelial function is becoming an important element of the global management of patients with RA, the mechanistic determinants of ED in RA are still poorly understood. Animal models of RA provide the unique opportunity to unravel the pathophysiological features of ED in RA. The present review summarizes the available data on mechanisms underlying ED in animal models of RA and proposes attractive prospects in order to discover novel therapeutic strategies of RA-associated ED. © 2014 Totoson et al.; licensee BioMed Central Ltd.


Senejoux F.,EA 4267 Fonctions et Dysfonctions epitheliales | Demougeot C.,EA 4267 Fonctions et Dysfonctions epitheliales | Karimov U.,CAS Xinjiang Technical Institute of Physics and Chemistry | Muyard F.,EA 4267 Fonctions et Dysfonctions epitheliales | And 3 more authors.
Biochemical Systematics and Ecology | Year: 2013

The present study constitutes the first phytochemical investigation of Echinops integrifolius Kar. & Kir. (Asteraceae). Four triterpenes, six flavonoids and one coumarin were isolated and identified. Among them, 6-methoxyflavones and 6-methoxyflavonols and the coumarin umbelliferone are reported from a species of Echinops for the first time. © 2012 Elsevier Ltd.


PubMed | EA 4267 Fonctions et Dysfonctions Epitheliales, Laboratoire Of Physiologie Animale and Université Ibn Tofail
Type: Journal Article | Journal: Journal of ethnopharmacology | Year: 2013

The stem bark of Terminalia superba (TS) is widely used as a decoction by Cameroonian folk medicine for the treatment of hypertension. The aim of the present study was to evaluate the effect of a chronic treatment with a TS extract on spontaneously hypertensive rats (SHR) with respect to efficacy, biochemical mechanisms and safety.Eleven-week-old SHR and normotensive Wistar Kyoto rats (WKY) were daily treated by gavage with a methylene chloride extract of stem bark of Terminalia superba (TMSE, 150mg/kg) or with the vehicle for 5 weeks. Systolic blood pressure (SBP) was measured weekly using the tail-cuff method. At the end of the treatment period, vascular function was assessed on isolated thoracic rings, urinary 8-iso-PGF2 levels were measured and cytochrome P-450 3A (CYP 3A) activity was evaluated in liver microsomes.TMSE reduced SBP (P<0.001) in SHR but not in WKY rats. In SHR, the vasorelaxant response to acetylcholine was significantly improved by TMSE as a result of increased nitric oxide synthase (NO) activity and decreased superoxide anion production. In addition, TMSE reduced the vasoconstrictive effect of phenylephrine and improved the sensitivity of smooth muscle cells to NO. TMSE dramatically decreased 8-iso-PGF2 levels in SHR. By contrast, TMSE did not affect all these parameters in WKY rats. Neither diuresis nor the hepatic CYP 3A activity was modified in both animal groups.This study demonstrated that Terminalia superba has a potent antihypertensive activity in SHR which is partly due to endothelium-dependent and endothelium-independent effects as well as decreased oxidative stress. The data also provide evidence for the lack of herb-drug interaction through hepatic CYP 3A.


PubMed | EA 4267 Fonctions et dysfonctions epitheliales and University Paris Saclay
Type: Journal Article | Journal: Magnesium research | Year: 2017

Obesity and related metabolic diseases are associated with increased risk of cardiovascular disease. We have previously shown the beneficial effects of dietary magnesium (Mg) supplementation on cardiovascular disease in rats. Therefore, we aimed to examine the effect of an Mg-deficient or supplemented diet on adipose tissue cellularity changes during aging, and on blood pressure (BP), in rats. Male rats received for one (young adult) or 22 months (old), an Mg-deficient (Def) (150mg/kg), standard (Std) (800mg/kg) or Mg-supplemented (Sup) (3200mg/kg) diet. Adipose tissue development and cellularity, BP and leptinemia were evaluated. In rats fed a standard diet, the large increase in adipose tissue weight observed during aging was related to an increase in both size and number of adipocytes. In young adult rats, although adiposity was unchanged, Mg supplementation resulted in a shift of the frequency distribution of adipocytes toward greater sizes, adipose cell weight increasing by 62%. Mg deficiency did not modify adipocyte size, but increased their number (30% more than for the standard or Sup-diet). In old rats, the Def-diet led to relative adipocyte hypotrophy, which was counterbalanced by an increase in the number of adipocyte. Conversely, adipocyte size and number were similar in the Sup-diet and standard diet-fed rats. BP was modified in old rats according to dietary Mg, whereas it remained unchanged young adult rats regardless of the diet received. This study suggests that Mg intake may affect age-related changes in rat adipose tissue lipid storage capacity.

Loading EA 4267 Fonctions et Dysfonctions Epitheliales collaborators
Loading EA 4267 Fonctions et Dysfonctions Epitheliales collaborators